过氧亚硝酸盐
药物输送
氧化应激
药理学
药品
材料科学
冲程(发动机)
缺血性中风
机制(生物学)
纳米技术
神经科学
中枢神经系统
医学
细胞存活
全身给药
癌症研究
下调和上调
作者
Xiao Liu,Xuehao Zhao,Heyu Pan,Hongmei Wu,Yangyang Jiang,Jiaxin Zheng,Yingxue Chang,Xing Su,Yumin Yang,Yong Ling
标识
DOI:10.1002/adfm.202524070
摘要
ABSTRACT Ischemic stroke (IS), with its high disability and mortality rates, remains a critical global health challenge, while current theranostic strategies fail to meet the demands of early diagnosis and timely intervention. Here, we report a breakthrough small‐molecule theranostic system ( ESL ) that integrates celastrol (Cel), a selective peroxynitrite (ONOO − )‐responsive trigger, and a hemicyanine‐based near‐infrared fluorophore. ESL undergoes a distinctive 1,4‐elimination reaction upon ONOO − activation, producing a 33‐fold fluorescence enhancement at 762 nm and enabling rapid visualization of ischemic lesions within 10 min. Therapeutically, ESL implements a dual‐mode strategy of instant scavenging and targeted delivery, simultaneously eliminating ONOO − ‐induced oxidative stress and releasing Cel to suppress neuroinflammation. This precise delivery markedly reduces systemic toxicity, achieving a superior safety profile compared with free Cel. Mechanistic studies further reveal that ESL inhibits the IL‐17/NF‐κB pathway, modulates microglial polarization, and suppresses pro‐inflammatory cytokines. Collectively, this work establishes an integrated “diagnosis–treatment–monitoring” paradigm for IS and provides a versatile platform for precision therapy of central nervous system disorders.
科研通智能强力驱动
Strongly Powered by AbleSci AI